TGF-β1 expression by glioma C6 cells in vitro

The aim of the work was to study the impact of fetal rat brain cell supernatant (FRBCS) on the expression of transforming growth factor β1 (TGF-β1) and p53 in C6 cells of rat glioma in vitro. Materials and Methods: FRBCS was obtained from suspensions of fetal rat brain cells on the 14th (E14) day of...

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Veröffentlicht in:Experimental Oncology
Datum:2017
Hauptverfasser: Liubich, L.D., Kovalevska, L.M., Lisyany, M.I., Semenova, V.M., Malysheva, T.A., Stayno, L.P., Vaslovych, V.V.
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Sprache:Englisch
Veröffentlicht: Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України 2017
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Online Zugang:https://nasplib.isofts.kiev.ua/handle/123456789/138583
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Zitieren:TGF-β1 expression by glioma C6 cells in vitro / L.D. Liubich, L.M. Kovalevska, M.I. Lisyany, V.M. Semenova, T.A. Malysheva, L.P. Stayno, V.V. Vaslovych // Experimental Oncology. — 2017 — Т. 39, № 4. — С. 258–263. — Бібліогр.: 40 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
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author Liubich, L.D.
Kovalevska, L.M.
Lisyany, M.I.
Semenova, V.M.
Malysheva, T.A.
Stayno, L.P.
Vaslovych, V.V.
author_facet Liubich, L.D.
Kovalevska, L.M.
Lisyany, M.I.
Semenova, V.M.
Malysheva, T.A.
Stayno, L.P.
Vaslovych, V.V.
citation_txt TGF-β1 expression by glioma C6 cells in vitro / L.D. Liubich, L.M. Kovalevska, M.I. Lisyany, V.M. Semenova, T.A. Malysheva, L.P. Stayno, V.V. Vaslovych // Experimental Oncology. — 2017 — Т. 39, № 4. — С. 258–263. — Бібліогр.: 40 назв. — англ.
collection DSpace DC
container_title Experimental Oncology
description The aim of the work was to study the impact of fetal rat brain cell supernatant (FRBCS) on the expression of transforming growth factor β1 (TGF-β1) and p53 in C6 cells of rat glioma in vitro. Materials and Methods: FRBCS was obtained from suspensions of fetal rat brain cells on the 14th (E14) day of gestation. C6 glioma cells were cultured for 48 h in the presence of FRBCS or FRBCS + anti-TGF-β1 monoclonal antibody. Immunocytochemical staining for TGF-β1 and p53 was performed. Results: The proportion of TGF-β1-immunopositive tumor cells in C6 glioma cultures was statistically significantly higher than in the control cell cultures of normal fetal rat brain. FRBCS reduced the proportion of TGF-β1-immunopositive tumor cells and increased the proportion of p53-immunopositive cells in C6 glioma cultures. In cells cultured with FRBCS + anti-TGF-β1 monoclonal antibody, the above effects of FRBCS were abrogated. Conclusion: The obtained results suggest that TGF-β1 seems to be responsible for decrease in TGF-β1 expression and increase in p53 expression in C6 glioma cells treated with FRBCS.
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publishDate 2017
publisher Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України
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spelling Liubich, L.D.
Kovalevska, L.M.
Lisyany, M.I.
Semenova, V.M.
Malysheva, T.A.
Stayno, L.P.
Vaslovych, V.V.
2018-06-19T10:00:39Z
2018-06-19T10:00:39Z
2017
TGF-β1 expression by glioma C6 cells in vitro / L.D. Liubich, L.M. Kovalevska, M.I. Lisyany, V.M. Semenova, T.A. Malysheva, L.P. Stayno, V.V. Vaslovych // Experimental Oncology. — 2017 — Т. 39, № 4. — С. 258–263. — Бібліогр.: 40 назв. — англ.
1812-9269
https://nasplib.isofts.kiev.ua/handle/123456789/138583
The aim of the work was to study the impact of fetal rat brain cell supernatant (FRBCS) on the expression of transforming growth factor β1 (TGF-β1) and p53 in C6 cells of rat glioma in vitro. Materials and Methods: FRBCS was obtained from suspensions of fetal rat brain cells on the 14th (E14) day of gestation. C6 glioma cells were cultured for 48 h in the presence of FRBCS or FRBCS + anti-TGF-β1 monoclonal antibody. Immunocytochemical staining for TGF-β1 and p53 was performed. Results: The proportion of TGF-β1-immunopositive tumor cells in C6 glioma cultures was statistically significantly higher than in the control cell cultures of normal fetal rat brain. FRBCS reduced the proportion of TGF-β1-immunopositive tumor cells and increased the proportion of p53-immunopositive cells in C6 glioma cultures. In cells cultured with FRBCS + anti-TGF-β1 monoclonal antibody, the above effects of FRBCS were abrogated. Conclusion: The obtained results suggest that TGF-β1 seems to be responsible for decrease in TGF-β1 expression and increase in p53 expression in C6 glioma cells treated with FRBCS.
en
Інститут експериментальної патології, онкології і радіобіології ім. Р.Є. Кавецького НАН України
Experimental Oncology
Original contributions
TGF-β1 expression by glioma C6 cells in vitro
Article
published earlier
spellingShingle TGF-β1 expression by glioma C6 cells in vitro
Liubich, L.D.
Kovalevska, L.M.
Lisyany, M.I.
Semenova, V.M.
Malysheva, T.A.
Stayno, L.P.
Vaslovych, V.V.
Original contributions
title TGF-β1 expression by glioma C6 cells in vitro
title_full TGF-β1 expression by glioma C6 cells in vitro
title_fullStr TGF-β1 expression by glioma C6 cells in vitro
title_full_unstemmed TGF-β1 expression by glioma C6 cells in vitro
title_short TGF-β1 expression by glioma C6 cells in vitro
title_sort tgf-β1 expression by glioma c6 cells in vitro
topic Original contributions
topic_facet Original contributions
url https://nasplib.isofts.kiev.ua/handle/123456789/138583
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